Fluorescence In Situ Hybridization Identifies Inversion 16 Masked by t(10;16)(q24;q22), t(7;16)(q21;q22), and t(2;16)(q37;q22) in Three Cases of AML-M4Eo
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference11 articles.
1. Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia;Le Beau;N Engl J Med,1983
2. Cancer Cytogenetics;Heim,1995
3. Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia;Liu;Blood,1995
4. Catalog of Chromosome Aberrations in Cancer;Mitelman,1994
5. Chromosome 16 and bone-marrow eosinophilia;De la Chapelle;N Engl J Med,1983
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1. Spectral karyotyping and fluorescence in situ hybridization analyses identified a novel three-way translocation involving inversion 16 in therapy-related acute myeloid leukemia M4eo;Cancer Genetics and Cytogenetics;2008-07
2. Granulocytic sarcoma of mesentery in acute myeloid leukemia with CBFB/MYH11 fusion gene but not inv(16) chromosome: Case report and review of literature;Leukemia Research;2006-08
3. Screening for core binding factor gene rearrangements in acute myeloid leukemia;Leukemia;2002-05
4. Chromosome 16 inversion-associated translocations in acute myeloid leukemia elucidated using a dual-color CBFB DNA probe;Cancer Genetics and Cytogenetics;2002-04
5. A novel variant three-way translocation of inversion 16 in a case of AML-M4eo following low dose methotrexate therapy;Cancer Genetics and Cytogenetics;2001-02
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